• Quality Control Senior Associate

    Actalent (Holly Springs, NC)


    Job Title: Quality Control Expert Associate

    Job Description

    This position is based 100% onsite in Holly Springs, NC, following a standard weekday schedule. The Quality Control Expert Associate will play a critical role in the startup and operations of the ANC facility, focusing on quality records management, including deviations, CAPAs, and change controls. The ideal candidate will have at least one year of experience in a GMP-regulated lab or manufacturing setting, with proficiency in the Veeva Quality system being highly desirable. Strong communication and grammar skills, along with a proactive, detail-oriented approach, are essential for success in this fast-paced environment.

    Responsibilities

    + Work collaboratively with Quality and Quality Assurance teams to author and own change control records and deviations in the DQMS Veeva System.

    + Lead investigation teams and help collect and report metrics for the systems team.

    + Assist with the review of validation documents to support equipment and computerized system onboarding.

    + Author, revise, and review documents and reports, including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, and technical reports.

    + Support the startup of a GMP QC laboratory.

    + Support routine activities over weekends and public holidays as required.

    Essential Skills

    + At least one year of experience in a GMP-regulated lab or manufacturing setting.

    + Strong writing and grammar skills.

    + Proficiency in Deviation and Change Control writing.

    + Experience with the Veeva Quality system.

    + Ability to lead meetings and drive investigations independently.

    + Proactive and detail-oriented.

    Additional Skills & Qualifications

    + High school/GED with 2 years of work experience, or Associates with 6 months of work experience, or Bachelors degree.

    + Leadership capabilities and practical aptitude.

    + Collaborative approach and proactive mindset.

    Work Environment

    This role requires working collaboratively with Quality and Quality Assurance teams onsite. The position includes authoring and owning change control records and deviations, leading investigation teams, and supporting the startup of a GMP QC laboratory. Routine activities may be required over weekends and public holidays, emphasizing a fast-paced and dynamic work setting.

    Pay and Benefits

    The pay range for this position is $38.00 - $43.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

    • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Holly Springs,NC.

     

    Application Deadline

     

    This position is anticipated to close on Aug 5, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.